Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9343 |
| ensemblid | ENSG00000108883.13 |
| hgncid | 30858 |
| symbol | EFTUD2 |
| name | elongation factor Tu GTP binding domain containing 2 |
| refseq_nuc | NM_004247.4 |
| refseq_prot | NP_004238.3 |
| ensembl_nuc | ENST00000426333.7 |
| ensembl_prot | ENSP00000392094.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 44849948 |
| end | 44899445 |
| strand | - |
| ver | v1.2 |
| region | chr17:44849948-44899445 |
| region5000 | chr17:44844948-44904445 |
| regionname0 | EFTUD2_chr17_44849948_44899445 |
| regionname5000 | EFTUD2_chr17_44844948_44904445 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 972 | 369 | 91 | 72 | 150 | 16 | 38 | 112 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | MDTDL others(967): Show |
chr17 | 44844948 | 44904445 |
| a0002 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | MDTDL others(967): Show |
chr17 | 44844948 | 44904445 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2916 | 293 | 71 | 60 | 120 | 10 | 30 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | ATGGA others(2911): Show |
chr17 | 44844948 | 44904445 | ||
| a0001c0002 | 0/0 | 2916 | 69 | 19 | 12 | 24 | 6 | 8 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | ATGGA others(2911): Show |
chr17 | 44844948 | 44904445 | ||
| a0001c0003 | 0/0 | 2916 | 2 | 0 | 0 | 2 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | ATGGA others(2911): Show |
chr17 | 44844948 | 44904445 | ||
| a0001c0005 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | ATGGA others(2911): Show |
chr17 | 44844948 | 44904445 | ||
| a0001c0006 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | ATGGA others(2911): Show |
chr17 | 44844948 | 44904445 | ||
| a0001c0007 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | ATGGA others(2911): Show |
chr17 | 44844948 | 44904445 | ||
| a0001c0008 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | ATGGA others(2911): Show |
chr17 | 44844948 | 44904445 | ||
| a0001c0009 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | ATGGA others(2911): Show |
chr17 | 44844948 | 44904445 | ||
| a0002c0004 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | ATGGA others(2911): Show |
chr17 | 44844948 | 44904445 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4326 | 61 | 28 | 7 | 13 | 0 | 13 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0002 | 1/0 | 4326 | 109 | 12 | 23 | 58 | 6 | 9 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0003 | 0/0 | 4326 | 60 | 11 | 9 | 33 | 1 | 6 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0004 | 0/0 | 4326 | 24 | 6 | 2 | 16 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0005 | 0/1 | 4326 | 18 | 3 | 12 | 0 | 1 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0006 | 0/0 | 4326 | 2 | 2 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0007 | 0/0 | 4326 | 7 | 7 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0008 | 0/0 | 4326 | 5 | 0 | 3 | 0 | 1 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0009 | 0/0 | 4326 | 2 | 0 | 1 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0010 | 0/0 | 4326 | 2 | 0 | 2 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0011 | 0/0 | 4326 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0012 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0001t0013 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0002t0001 | 0/0 | 4326 | 59 | 16 | 10 | 23 | 6 | 4 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0002t0002 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0002t0004 | 0/0 | 4326 | 3 | 3 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0002t0006 | 0/0 | 4326 | 6 | 0 | 2 | 0 | 0 | 4 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0003t0001 | 0/0 | 4326 | 2 | 0 | 0 | 2 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0005t0003 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0006t0002 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0007t0001 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0008t0002 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0001c0009t0003 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| a0002c0004t0001 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | GCAGG others(4321): Show |
chr17 | 44844948 | 44904445 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0001 | 0/0 | 10 | 0 | 2 | 7 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0100 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0009g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0010g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0011g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0001t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0002t0006g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0005t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0006t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0007t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0008t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0001c0009t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| a0002c0004t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | GBR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00099 | hp2 | a0001 | c0001 | t0008 | g0028 | EUR | GBR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | GBR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0275 | EUR | GBR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0118 | EUR | FIN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0131 | EUR | FIN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0249 | EUR | FIN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0011 | EUR | FIN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00639 | hp2 | a0001 | c0002 | t0006 | g0168 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00642 | hp2 | a0001 | c0001 | t0010 | g0189 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | CHS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0251 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00741 | hp1 | a0001 | c0001 | t0011 | g0165 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0188 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0255 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0252 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01081 | hp1 | a0001 | c0002 | t0006 | g0170 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0256 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01099 | hp2 | a0001 | c0001 | t0009 | g0130 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0333 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0254 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0037 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0036 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0245 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0250 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0330 | AMR | PUR | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0291 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0246 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0032 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0026 | EUR | IBS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0068 | EUR | IBS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0087 | EUR | IBS | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0302 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0312 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0265 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0248 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0319 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | CDX | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | CDX | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CDX | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CDX | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0274 | AMR | PEL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | KHV | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0331 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0321 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02735 | hp1 | a0001 | c0002 | t0006 | g0253 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0247 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0258 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0329 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0158 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02970 | hp2 | a0002 | c0004 | t0001 | g0338 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0327 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0337 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0323 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03139 | hp2 | a0001 | c0002 | t0004 | g0325 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0237 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03209 | hp1 | a0001 | c0007 | t0001 | g0025 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0160 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03486 | hp2 | a0001 | c0002 | t0004 | g0326 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03490 | hp2 | a0001 | c0002 | t0006 | g0167 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03492 | hp1 | a0001 | c0002 | t0006 | g0169 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0334 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | ESN | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0332 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0324 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0020 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03669 | hp1 | a0001 | c0001 | t0008 | g0030 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0271 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | BEB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03834 | hp2 | a0001 | c0002 | t0006 | g0171 | SAS | BEB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0268 | SAS | BEB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | STU | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | YRI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0328 | AFR | YRI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18747 | hp2 | a0001 | c0006 | t0002 | g0145 | EAS | CHB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | YRI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18948 | hp2 | a0001 | c0005 | t0003 | g0266 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18952 | hp2 | a0001 | c0009 | t0003 | g0272 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | LWK | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0154 | AFR | LWK | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19058 | hp1 | a0001 | c0008 | t0002 | g0094 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0232 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0166 | AFR | YRI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ASW | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ASW | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0119 | EUR | TSI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0088 | EUR | TSI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | TSI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | TSI | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0277 | SAS | GIH | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | GIH | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0335 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0257 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0336 | AFR | MSL | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | LWK | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0244 | REF | REF | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0100 | REF | REF | EFTUD2_chr17_44844948_44904445 | EFTUD2 | chr17 | 44844948 | 44904445 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44859151 | C | T | 1 | a0002 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1891G>A | p.Gly631Ser | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/28 | 1972/4326 | 1891/2919 | 631/972 | chr17 | 44859151 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44852493 | G | A | 1 | a0001c0005 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.2631C>T | p.Ala877Ala | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 26/28 | 2712/4326 | 2631/2919 | 877/972 | chr17 | 44852493 | |||
| chr17:44854962 | C | A | 1 | a0001c0006 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.2088G>T | p.Leu696Leu | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 21/28 | 2169/4326 | 2088/2919 | 696/972 | chr17 | 44854962 | |||
| chr17:44862715 | G | A | 1 | a0001c0003 | 2 | HG02083.hp1 NA19083.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1605C>T | p.Ala535Ala | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/28 | 1686/4326 | 1605/2919 | 535/972 | chr17 | 44862715 | |||
| chr17:44862745 | G | A | 1 | a0001c0007 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1575C>T | p.Cys525Cys | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/28 | 1656/4326 | 1575/2919 | 525/972 | chr17 | 44862745 | |||
| chr17:44864967 | G | A | 1 | a0001c0008 | 1 | NA19058.hp1 | synonymous_variant | LOW | c.1248C>T | p.Leu416Leu | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/28 | 1329/4326 | 1248/2919 | 416/972 | chr17 | 44864967 | |||
| chr17:44872456 | G | A | 1 | a0001c0009 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.984C>T | p.Ala328Ala | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/28 | 1065/4326 | 984/2919 | 328/972 | chr17 | 44872456 | |||
| chr17:44876041 | A | G | 2 | a0001c0002 a0002c0004 |
70 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(67): Show |
synonymous_variant | LOW | c.762T>C | p.Thr254Thr | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/28 | 843/4326 | 762/2919 | 254/972 | chr17 | 44876041 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44850186 | C | T | 1 | a0001c0001t0013 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1088G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 1088 | chr17 | 44850186 | ||||||
| chr17:44850260 | A | G | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*1014T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 1014 | chr17 | 44850260 | ||||||
| chr17:44850282 | C | T | 2 | a0001c0001t0006 a0001c0002t0006 |
8 | HG00639.hp2 HG01081.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*992G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 992 | chr17 | 44850282 | ||||||
| chr17:44850353 | G | A | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(3): Show |
57 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*921C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 921 | chr17 | 44850353 | ||||||
| chr17:44850355 | G | A | 1 | a0001c0001t0009 | 2 | HG00280.hp2 HG01099.hp2 |
3_prime_UTR_variant | MODIFIER | c.*919C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 919 | chr17 | 44850355 | ||||||
| chr17:44850379 | G | A | 1 | a0001c0001t0012 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*895C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 895 | chr17 | 44850379 | ||||||
| chr17:44850488 | T | G | 1 | a0001c0001t0013 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*786A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 786 | chr17 | 44850488 | ||||||
| chr17:44850597 | G | A | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(3): Show |
94 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*677C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 677 | chr17 | 44850597 | ||||||
| chr17:44850618 | T | C | 1 | a0001c0001t0010 | 2 | HG00642.hp2 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*656A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 656 | chr17 | 44850618 | ||||||
| chr17:44850686 | T | C | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(13): Show |
246 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*588A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 588 | chr17 | 44850686 | ||||||
| chr17:44850832 | C | T | 1 | a0001c0001t0008 | 5 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*442G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 442 | chr17 | 44850832 | ||||||
| chr17:44850870 | C | T | 1 | a0001c0001t0011 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 28/28 | 404 | chr17 | 44850870 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44851675 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2823+35C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 27/27 | chr17 | 44851675 | |||||||
| chr17:44852051 | G | A | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2716-234C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 26/27 | chr17 | 44852051 | |||||||
| chr17:44852192 | C | T | 1 | a0001c0001t0003g0274 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2715+217G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 26/27 | chr17 | 44852192 | |||||||
| chr17:44852213 | G | A | 1 | a0001c0002t0001g0026 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2715+196C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 26/27 | chr17 | 44852213 | |||||||
| chr17:44852222 | A | C | 1 | a0001c0001t0003g0286 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2715+187T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 26/27 | chr17 | 44852222 | |||||||
| chr17:44852226 | CT | C | 9 | a0001c0001t0001g0064 a0001c0001t0002g0126 a0001c0001t0002g0151 others(6): Show |
9 | HG00639.hp2 HG01169.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.2715+182delA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 26/27 | chr17 | 44852226 | |||||||
| chr17:44852291 | G | C | 7 | a0001c0001t0006g0005 a0001c0002t0006g0167 a0001c0002t0006g0168 others(4): Show |
8 | HG00639.hp2 HG01081.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2715+118C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 26/27 | chr17 | 44852291 | |||||||
| chr17:44852391 | C | G | 5 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0068 others(2): Show |
7 | HG00323.hp2 HG01255.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.2715+18G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 26/27 | chr17 | 44852391 | |||||||
| chr17:44852602 | T | C | 232 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(229): Show |
247 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.2562-40A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 25/27 | chr17 | 44852602 | |||||||
| chr17:44852617 | G | T | 22 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(19): Show |
25 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.2562-55C>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 25/27 | chr17 | 44852617 | |||||||
| chr17:44852701 | A | G | 5 | a0001c0001t0003g0281 a0001c0001t0003g0283 a0001c0001t0003g0289 others(2): Show |
5 | HG00544.hp1 HG00621.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.2562-139T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 25/27 | chr17 | 44852701 | |||||||
| chr17:44852878 | A | C | 61 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0003g0262 others(58): Show |
61 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2562-316T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 25/27 | chr17 | 44852878 | |||||||
| chr17:44852886 | A | AT | 224 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(221): Show |
239 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2562-325dupA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 25/27 | chr17 | 44852886 | |||||||
| chr17:44852886 | A | ATT | 6 | a0001c0001t0001g0234 a0001c0001t0004g0041 a0001c0001t0005g0247 others(3): Show |
6 | HG00597.hp2 HG02523.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2562-326_2562-325d others(4): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 25/27 | chr17 | 44852886 | |||||||
| chr17:44853030 | G | C | 1 | a0001c0001t0002g0209 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2561+266C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 25/27 | chr17 | 44853030 | |||||||
| chr17:44853190 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2561+106C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 25/27 | chr17 | 44853190 | |||||||
| chr17:44853241 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2561+55G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 25/27 | chr17 | 44853241 | |||||||
| chr17:44853456 | C | T | 1 | a0001c0001t0003g0291 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2466+61G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 24/27 | chr17 | 44853456 | |||||||
| chr17:44853491 | G | A | 41 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(38): Show |
48 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.2466+26C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 24/27 | chr17 | 44853491 | |||||||
| chr17:44853874 | G | A | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2348-239C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 23/27 | chr17 | 44853874 | |||||||
| chr17:44854068 | A | C | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2347+201T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 23/27 | chr17 | 44854068 | |||||||
| chr17:44854120 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2347+149C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 23/27 | chr17 | 44854120 | |||||||
| chr17:44854213 | A | G | 1 | a0001c0002t0002g0174 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2347+56T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 23/27 | chr17 | 44854213 | |||||||
| chr17:44854376 | C | A | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2260-20G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 22/27 | chr17 | 44854376 | |||||||
| chr17:44854386 | G | A | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2260-30C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 22/27 | chr17 | 44854386 | |||||||
| chr17:44854395 | G | C | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2260-39C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 22/27 | chr17 | 44854395 | |||||||
| chr17:44854416 | GGGA | G | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2260-63_2260-61del others(3): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 22/27 | chr17 | 44854416 | |||||||
| chr17:44854825 | C | T | 15 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(12): Show |
17 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.2132+93G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 21/27 | chr17 | 44854825 | |||||||
| chr17:44854876 | C | T | 55 | a0001c0001t0001g0339 a0001c0001t0001g0340 a0001c0002t0001g0003 others(52): Show |
63 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2132+42G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 21/27 | chr17 | 44854876 | |||||||
| chr17:44854889 | C | T | 1 | a0001c0001t0003g0322 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2132+29G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 21/27 | chr17 | 44854889 | |||||||
| chr17:44854898 | C | A | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2132+20G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 21/27 | chr17 | 44854898 | |||||||
| chr17:44855083 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2046-79G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855083 | |||||||
| chr17:44855106 | A | G | 111 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0197 others(108): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.2046-102T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855106 | |||||||
| chr17:44855337 | C | T | 1 | a0001c0001t0005g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2046-333G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855337 | |||||||
| chr17:44855359 | G | A | 1 | a0001c0001t0007g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2046-355C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855359 | |||||||
| chr17:44855428 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2046-424C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855428 | |||||||
| chr17:44855467 | T | C | 1 | a0001c0001t0003g0116 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2046-463A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855467 | |||||||
| chr17:44855545 | C | T | 1 | a0001c0002t0001g0085 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2046-541G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855545 | |||||||
| chr17:44855773 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0138 |
2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2046-769T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855773 | |||||||
| chr17:44855952 | T | G | 2 | a0001c0001t0003g0263 a0001c0001t0003g0269 |
2 | NA19068.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2046-948A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855952 | |||||||
| chr17:44855958 | G | GA | 95 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0163 others(92): Show |
105 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.2046-955dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44855958 | |||||||
| chr17:44856130 | C | CA | 140 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0182 others(137): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.2045+944dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856130 | |||||||
| chr17:44856130 | C | CAA | 20 | a0001c0001t0001g0220 a0001c0001t0001g0223 a0001c0001t0002g0136 others(17): Show |
20 | HG00438.hp2 HG01175.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.2045+943_2045+944d others(4): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856130 | |||||||
| chr17:44856130 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2045+933_2045+944d others(14): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856130 | |||||||
| chr17:44856258 | G | A | 6 | a0001c0002t0006g0167 a0001c0002t0006g0168 a0001c0002t0006g0169 others(3): Show |
6 | HG00639.hp2 HG01081.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2045+817C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856258 | |||||||
| chr17:44856299 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2045+776G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856299 | |||||||
| chr17:44856396 | G | C | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2045+679C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856396 | |||||||
| chr17:44856519 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2045+556C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856519 | |||||||
| chr17:44856758 | C | CA | 129 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0059 others(126): Show |
142 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.2045+316dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856758 | |||||||
| chr17:44856758 | C | CAA | 14 | a0001c0001t0001g0185 a0001c0001t0001g0192 a0001c0001t0001g0196 others(11): Show |
14 | HG01261.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2045+315_2045+316d others(4): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856758 | |||||||
| chr17:44856773 | C | A | 2 | a0001c0002t0006g0168 a0001c0002t0006g0170 |
2 | HG00639.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2045+302G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856773 | |||||||
| chr17:44856816 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2045+259T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856816 | |||||||
| chr17:44856848 | T | G | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2045+227A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856848 | |||||||
| chr17:44856955 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2045+120A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44856955 | |||||||
| chr17:44857004 | A | G | 253 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(250): Show |
268 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.2045+71T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44857004 | |||||||
| chr17:44857047 | T | C | 57 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(54): Show |
60 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.2045+28A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 20/27 | chr17 | 44857047 | |||||||
| chr17:44857311 | A | G | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1963-154T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857311 | |||||||
| chr17:44857326 | T | C | 251 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(248): Show |
266 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.1963-169A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857326 | |||||||
| chr17:44857523 | A | G | 1 | a0001c0002t0001g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1963-366T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857523 | |||||||
| chr17:44857645 | T | C | 1 | a0001c0002t0001g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1963-488A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857645 | |||||||
| chr17:44857687 | G | A | 21 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0183 others(18): Show |
21 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1963-530C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857687 | |||||||
| chr17:44857691 | T | C | 104 | a0001c0001t0001g0065 a0001c0001t0001g0177 a0001c0001t0001g0179 others(101): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1963-534A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857691 | |||||||
| chr17:44857841 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1963-684A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857841 | |||||||
| chr17:44857920 | C | CT | 11 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0002g0108 others(8): Show |
11 | HG01361.hp1 HG02074.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1963-764dupA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857920 | |||||||
| chr17:44857920 | C | CTTTTTT | 15 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(12): Show |
18 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1963-769_1963-764d others(8): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857920 | |||||||
| chr17:44857920 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0064 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1963-772_1963-764d others(11): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857920 | |||||||
| chr17:44857920 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0093 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1963-773_1963-764d others(12): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857920 | |||||||
| chr17:44857931 | T | C | 1 | a0001c0001t0007g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1963-774A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857931 | |||||||
| chr17:44857953 | G | A | 17 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(14): Show |
20 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1963-796C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44857953 | |||||||
| chr17:44858045 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1963-888G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858045 | |||||||
| chr17:44858169 | G | A | 12 | a0001c0001t0001g0163 a0001c0001t0001g0183 a0001c0001t0001g0191 others(9): Show |
12 | HG00621.hp1 HG00639.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.1962+911C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858169 | |||||||
| chr17:44858170 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0185 a0001c0001t0001g0186 |
4 | HG02258.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1962+910G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858170 | |||||||
| chr17:44858261 | G | A | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1962+819C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858261 | |||||||
| chr17:44858321 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1962+759C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858321 | |||||||
| chr17:44858336 | A | C | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1962+744T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858336 | |||||||
| chr17:44858359 | C | T | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1962+721G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858359 | |||||||
| chr17:44858456 | G | C | 18 | a0001c0001t0001g0163 a0001c0001t0001g0183 a0001c0001t0001g0191 others(15): Show |
18 | HG00621.hp1 HG00639.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1962+624C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858456 | |||||||
| chr17:44858553 | G | C | 1 | a0001c0002t0001g0332 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1962+527C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858553 | |||||||
| chr17:44858623 | G | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1962+457C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858623 | |||||||
| chr17:44858635 | G | C | 66 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(63): Show |
66 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1962+445C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858635 | |||||||
| chr17:44858661 | G | C | 1 | a0001c0001t0003g0273 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1962+419C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858661 | |||||||
| chr17:44858667 | A | C | 2 | a0001c0001t0003g0286 a0001c0001t0003g0295 |
2 | NA18940.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1962+413T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858667 | |||||||
| chr17:44858751 | T | C | 1 | a0001c0001t0002g0044 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1962+329A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858751 | |||||||
| chr17:44858918 | C | A | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1962+162G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 19/27 | chr17 | 44858918 | |||||||
| chr17:44859327 | AG | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1861-147delC | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859327 | |||||||
| chr17:44859428 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1861-247A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859428 | |||||||
| chr17:44859434 | T | C | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1861-253A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859434 | |||||||
| chr17:44859478 | C | A | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1861-297G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859478 | |||||||
| chr17:44859540 | A | T | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1861-359T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859540 | |||||||
| chr17:44859641 | G | GCA | 61 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(58): Show |
69 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1860+262_1860+263d others(4): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859641 | |||||||
| chr17:44859641 | G | GCACA | 8 | a0001c0001t0007g0154 a0001c0001t0007g0155 a0001c0001t0007g0156 others(5): Show |
8 | HG02055.hp1 HG02723.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1860+260_1860+263d others(6): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859641 | |||||||
| chr17:44859641 | G | GCACACA | 4 | a0001c0002t0001g0329 a0001c0002t0001g0333 a0001c0002t0001g0335 others(1): Show |
4 | HG01109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1860+258_1860+263d others(8): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859641 | |||||||
| chr17:44859641 | G | GCACACAC others(1): Show |
7 | a0001c0002t0001g0324 a0001c0002t0001g0327 a0001c0002t0001g0328 others(4): Show |
7 | HG01243.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1860+256_1860+263d others(10): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859641 | |||||||
| chr17:44859674 | ACCC | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1860+228_1860+230d others(5): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859674 | |||||||
| chr17:44859737 | C | T | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1860+168G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859737 | |||||||
| chr17:44859772 | C | T | 6 | a0001c0001t0003g0260 a0001c0001t0003g0270 a0001c0001t0003g0280 others(3): Show |
6 | HG01169.hp1 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1860+133G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859772 | |||||||
| chr17:44859803 | G | A | 32 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(29): Show |
33 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1860+102C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859803 | |||||||
| chr17:44859837 | G | A | 1 | a0001c0001t0005g0248 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1860+68C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859837 | |||||||
| chr17:44859854 | A | T | 1 | a0001c0001t0002g0117 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1860+51T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 18/27 | chr17 | 44859854 | |||||||
| chr17:44860091 | G | A | 1 | a0001c0001t0002g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1720-46C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 17/27 | chr17 | 44860091 | |||||||
| chr17:44860178 | G | C | 2 | a0001c0001t0003g0296 a0001c0001t0003g0305 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1720-133C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 17/27 | chr17 | 44860178 | |||||||
| chr17:44860253 | C | A | 1 | a0001c0002t0001g0087 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1719+179G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 17/27 | chr17 | 44860253 | |||||||
| chr17:44860305 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1719+127T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 17/27 | chr17 | 44860305 | |||||||
| chr17:44860381 | C | G | 17 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(14): Show |
20 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1719+51G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 17/27 | chr17 | 44860381 | |||||||
| chr17:44860413 | G | A | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1719+19C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 17/27 | chr17 | 44860413 | |||||||
| chr17:44860595 | A | AT | 71 | a0001c0001t0001g0190 a0001c0001t0001g0196 a0001c0001t0001g0215 others(68): Show |
71 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1608-53dupA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44860595 | |||||||
| chr17:44860595 | AT | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0060 others(18): Show |
22 | HG01070.hp1 HG01099.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1608-53delA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44860595 | |||||||
| chr17:44860883 | G | A | 5 | a0001c0001t0002g0136 a0001c0001t0002g0140 a0001c0001t0002g0204 others(2): Show |
5 | HG00140.hp1 HG01361.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1608-340C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44860883 | |||||||
| chr17:44860928 | T | G | 1 | a0001c0001t0003g0277 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1608-385A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44860928 | |||||||
| chr17:44860959 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1608-416T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44860959 | |||||||
| chr17:44861196 | T | C | 2 | a0001c0001t0003g0286 a0001c0001t0003g0295 |
2 | NA18940.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1608-653A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861196 | |||||||
| chr17:44861432 | G | GA | 13 | a0001c0001t0001g0182 a0001c0001t0001g0193 a0001c0001t0001g0194 others(10): Show |
13 | HG00280.hp2 HG00621.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1608-890dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861432 | |||||||
| chr17:44861432 | GA | G | 135 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0059 others(132): Show |
141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1608-890delT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861432 | |||||||
| chr17:44861432 | GAA | G | 49 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0008 others(46): Show |
56 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1608-891_1608-890d others(4): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861432 | |||||||
| chr17:44861583 | A | T | 1 | a0001c0001t0001g0194 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1608-1040T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861583 | |||||||
| chr17:44861588 | C | G | 6 | a0001c0001t0003g0261 a0001c0001t0003g0265 a0001c0001t0003g0271 others(3): Show |
6 | HG00140.hp2 HG01943.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608-1045G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861588 | |||||||
| chr17:44861602 | G | T | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1608-1059C>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861602 | |||||||
| chr17:44861733 | CA | C | 7 | a0001c0001t0007g0154 a0001c0001t0007g0155 a0001c0001t0007g0156 others(4): Show |
7 | HG02055.hp1 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1607+979delT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861733 | |||||||
| chr17:44861760 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1607+953G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861760 | |||||||
| chr17:44861802 | G | A | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1607+911C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861802 | |||||||
| chr17:44861821 | A | G | 95 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(92): Show |
98 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1607+892T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861821 | |||||||
| chr17:44861858 | G | A | 1 | a0001c0001t0010g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1607+855C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861858 | |||||||
| chr17:44861969 | G | A | 5 | a0001c0002t0001g0026 a0001c0002t0001g0087 a0001c0002t0001g0088 others(2): Show |
5 | HG00642.hp1 HG00741.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1607+744C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44861969 | |||||||
| chr17:44862012 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1607+701T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862012 | |||||||
| chr17:44862098 | T | C | 3 | a0001c0002t0001g0015 a0001c0002t0001g0236 a0001c0002t0001g0237 |
4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1607+615A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862098 | |||||||
| chr17:44862218 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1607+495A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862218 | |||||||
| chr17:44862237 | C | T | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1607+476G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862237 | |||||||
| chr17:44862260 | C | T | 1 | a0001c0001t0004g0046 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1607+453G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862260 | |||||||
| chr17:44862262 | T | C | 16 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(13): Show |
19 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1607+451A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862262 | |||||||
| chr17:44862373 | C | G | 1 | a0001c0001t0003g0290 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1607+340G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862373 | |||||||
| chr17:44862427 | C | G | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1607+286G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862427 | |||||||
| chr17:44862585 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1607+128C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862585 | |||||||
| chr17:44862599 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0222 others(2): Show |
6 | HG01884.hp2 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1607+114G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862599 | |||||||
| chr17:44862691 | C | T | 40 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0163 others(37): Show |
42 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1607+22G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 16/27 | chr17 | 44862691 | |||||||
| chr17:44862920 | C | A | 2 | a0001c0001t0001g0199 a0001c0001t0013g0166 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1414-14G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44862920 | |||||||
| chr17:44863049 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0190 |
2 | NA19002.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1414-143G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863049 | |||||||
| chr17:44863079 | G | A | 1 | a0001c0001t0003g0316 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1414-173C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863079 | |||||||
| chr17:44863102 | TCTC | T | 79 | a0001c0001t0001g0311 a0001c0001t0003g0261 a0001c0001t0003g0262 others(76): Show |
82 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1414-199_1414-197d others(5): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863102 | |||||||
| chr17:44863105 | CCT | C | 4 | a0001c0001t0003g0260 a0001c0001t0003g0287 a0001c0003t0001g0176 others(1): Show |
4 | HG01891.hp1 HG02083.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414-201_1414-200d others(4): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863105 | |||||||
| chr17:44863108 | C | T | 2 | a0001c0001t0003g0260 a0001c0001t0003g0287 |
2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1414-202G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863108 | |||||||
| chr17:44863151 | C | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1414-245G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863151 | |||||||
| chr17:44863178 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1414-272A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863178 | |||||||
| chr17:44863233 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0013g0166 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1414-327T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863233 | |||||||
| chr17:44863289 | T | C | 1 | a0001c0002t0001g0026 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1413+366A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863289 | |||||||
| chr17:44863372 | G | A | 1 | a0001c0001t0003g0308 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1413+283C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863372 | |||||||
| chr17:44863410 | C | T | 9 | a0001c0002t0001g0015 a0001c0002t0001g0236 a0001c0002t0001g0237 others(6): Show |
10 | HG00639.hp2 HG01081.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1413+245G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863410 | |||||||
| chr17:44863504 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1413+151T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863504 | |||||||
| chr17:44863583 | G | A | 2 | a0001c0001t0003g0263 a0001c0001t0003g0269 |
2 | NA19068.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1413+72C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 15/27 | chr17 | 44863583 | |||||||
| chr17:44863880 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1286-98G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44863880 | |||||||
| chr17:44863995 | G | A | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1286-213C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44863995 | |||||||
| chr17:44864080 | C | T | 1 | a0001c0001t0003g0289 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1286-298G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864080 | |||||||
| chr17:44864089 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1286-307C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864089 | |||||||
| chr17:44864100 | T | C | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1286-318A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864100 | |||||||
| chr17:44864149 | C | A | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1286-367G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864149 | |||||||
| chr17:44864152 | G | A | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1286-370C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864152 | |||||||
| chr17:44864321 | G | A | 1 | a0001c0001t0003g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1286-539C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864321 | |||||||
| chr17:44864339 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1286-557G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864339 | |||||||
| chr17:44864354 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1286-572C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864354 | |||||||
| chr17:44864842 | C | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1285+88G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864842 | |||||||
| chr17:44864852 | G | A | 1 | a0001c0002t0001g0011 | 2 | HG00323.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1285+78C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864852 | |||||||
| chr17:44864871 | T | A | 3 | a0001c0001t0002g0113 a0001c0001t0002g0124 a0001c0001t0002g0132 |
3 | HG00558.hp2 NA19064.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1285+59A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 14/27 | chr17 | 44864871 | |||||||
| chr17:44865288 | CCAATAAA others(5): Show |
C | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1150-235_1150-224d others(14): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44865288 | |||||||
| chr17:44865381 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1150-316T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44865381 | |||||||
| chr17:44865387 | C | T | 238 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(235): Show |
253 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.1150-322G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44865387 | |||||||
| chr17:44865450 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1150-385T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44865450 | |||||||
| chr17:44865697 | T | C | 1 | a0001c0001t0005g0250 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1150-632A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44865697 | |||||||
| chr17:44865723 | C | T | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1150-658G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44865723 | |||||||
| chr17:44865990 | C | T | 4 | a0001c0001t0001g0199 a0001c0001t0002g0135 a0001c0001t0002g0139 others(1): Show |
4 | HG03195.hp1 HG03453.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-925G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44865990 | |||||||
| chr17:44866065 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1150-1000G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866065 | |||||||
| chr17:44866355 | T | C | 1 | a0001c0001t0004g0321 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1150-1290A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866355 | |||||||
| chr17:44866408 | T | C | 1 | a0001c0001t0010g0188 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1150-1343A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866408 | |||||||
| chr17:44866411 | A | ATTTAT | 95 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(92): Show |
98 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1150-1351_1150-134 others(9): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866411 | |||||||
| chr17:44866551 | G | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149+1256C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866551 | |||||||
| chr17:44866621 | C | T | 61 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0003g0262 others(58): Show |
61 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1149+1186G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866621 | |||||||
| chr17:44866781 | C | T | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1149+1026G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866781 | |||||||
| chr17:44866850 | G | T | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1149+957C>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866850 | |||||||
| chr17:44866944 | A | G | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1149+863T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866944 | |||||||
| chr17:44866972 | T | C | 17 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(14): Show |
20 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1149+835A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866972 | |||||||
| chr17:44866997 | C | T | 3 | a0001c0001t0002g0136 a0001c0001t0002g0204 a0001c0001t0002g0207 |
3 | HG00140.hp1 HG01361.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1149+810G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44866997 | |||||||
| chr17:44867147 | CAGG | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(1): Show |
4 | NA18980.hp1 NA18983.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149+657_1149+659d others(5): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867147 | |||||||
| chr17:44867217 | A | G | 2 | a0001c0001t0003g0263 a0001c0001t0003g0269 |
2 | NA19068.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1149+590T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867217 | |||||||
| chr17:44867223 | C | T | 37 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0008 others(34): Show |
44 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1149+584G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867223 | |||||||
| chr17:44867297 | A | AT | 16 | a0001c0001t0001g0184 a0001c0001t0002g0023 a0001c0001t0002g0114 others(13): Show |
17 | HG00558.hp2 HG00642.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1149+509dupA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867297 | |||||||
| chr17:44867297 | A | ATT | 88 | a0001c0001t0001g0056 a0001c0001t0001g0311 a0001c0001t0002g0033 others(85): Show |
89 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1149+508_1149+509d others(4): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867297 | |||||||
| chr17:44867297 | A | ATTT | 7 | a0001c0001t0003g0276 a0001c0001t0003g0281 a0001c0001t0003g0287 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149+507_1149+509d others(5): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867297 | |||||||
| chr17:44867297 | AT | A | 10 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0064 others(7): Show |
10 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1149+509delA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867297 | |||||||
| chr17:44867339 | G | A | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1149+468C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867339 | |||||||
| chr17:44867448 | C | T | 1 | a0001c0002t0001g0071 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1149+359G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867448 | |||||||
| chr17:44867459 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1149+348G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867459 | |||||||
| chr17:44867678 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1149+129T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867678 | |||||||
| chr17:44867700 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1149+107C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867700 | |||||||
| chr17:44867704 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1149+103A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 13/27 | chr17 | 44867704 | |||||||
| chr17:44867928 | A | G | 238 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(235): Show |
253 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.1059-31T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 12/27 | chr17 | 44867928 | |||||||
| chr17:44867931 | G | A | 1 | a0001c0002t0006g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1059-34C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 12/27 | chr17 | 44867931 | |||||||
| chr17:44867944 | T | C | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1059-47A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 12/27 | chr17 | 44867944 | |||||||
| chr17:44868173 | T | TA | 51 | a0001c0001t0002g0017 a0001c0001t0002g0033 a0001c0001t0002g0040 others(48): Show |
54 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1058+113dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 12/27 | chr17 | 44868173 | |||||||
| chr17:44868174 | A | T | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1058+113T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 12/27 | chr17 | 44868174 | |||||||
| chr17:44868257 | C | A | 1 | a0001c0001t0004g0321 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1058+30G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 12/27 | chr17 | 44868257 | |||||||
| chr17:44868395 | G | A | 2 | a0001c0001t0002g0062 a0001c0002t0001g0243 |
2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.995-45C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44868395 | |||||||
| chr17:44868498 | G | A | 1 | a0001c0001t0003g0295 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.995-148C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44868498 | |||||||
| chr17:44868499 | A | G | 254 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(251): Show |
270 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.995-149T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44868499 | |||||||
| chr17:44869021 | T | A | 5 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0200 others(2): Show |
5 | HG02083.hp1 NA18944.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.995-671A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869021 | |||||||
| chr17:44869246 | G | A | 3 | a0001c0001t0002g0105 a0001c0001t0002g0109 a0001c0001t0002g0110 |
3 | HG00408.hp1 HG02027.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.995-896C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869246 | |||||||
| chr17:44869515 | G | C | 5 | a0001c0001t0008g0028 a0001c0001t0008g0030 a0001c0001t0008g0032 others(2): Show |
5 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1165C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869515 | |||||||
| chr17:44869659 | A | C | 5 | a0001c0001t0003g0260 a0001c0001t0003g0270 a0001c0001t0003g0280 others(2): Show |
5 | HG01169.hp1 HG01891.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.995-1309T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869659 | |||||||
| chr17:44869681 | T | C | 1 | a0001c0001t0013g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.995-1331A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869681 | |||||||
| chr17:44869703 | G | C | 6 | a0001c0002t0006g0167 a0001c0002t0006g0168 a0001c0002t0006g0169 others(3): Show |
6 | HG00639.hp2 HG01081.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-1353C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869703 | |||||||
| chr17:44869719 | A | C | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.995-1369T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869719 | |||||||
| chr17:44869721 | T | C | 7 | a0001c0001t0007g0154 a0001c0001t0007g0155 a0001c0001t0007g0156 others(4): Show |
7 | HG02055.hp1 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.995-1371A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869721 | |||||||
| chr17:44869746 | T | C | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.995-1396A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869746 | |||||||
| chr17:44869946 | T | C | 16 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(13): Show |
19 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.995-1596A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44869946 | |||||||
| chr17:44870333 | AC | A | 17 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(14): Show |
20 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.995-1984delG | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870333 | |||||||
| chr17:44870381 | T | C | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.995-2031A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870381 | |||||||
| chr17:44870518 | G | A | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.994+1928C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870518 | |||||||
| chr17:44870594 | C | T | 1 | a0001c0001t0003g0288 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.994+1852G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870594 | |||||||
| chr17:44870613 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.994+1833G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870613 | |||||||
| chr17:44870794 | C | T | 1 | a0001c0002t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.994+1652G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870794 | |||||||
| chr17:44870866 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.994+1580T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870866 | |||||||
| chr17:44870896 | T | C | 1 | a0001c0001t0002g0017 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.994+1550A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870896 | |||||||
| chr17:44870901 | C | T | 61 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0003g0262 others(58): Show |
61 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.994+1545G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870901 | |||||||
| chr17:44870972 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.994+1474G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44870972 | |||||||
| chr17:44871007 | G | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.994+1439C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871007 | |||||||
| chr17:44871017 | C | CA | 35 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(32): Show |
37 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.994+1428dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871017 | |||||||
| chr17:44871165 | G | C | 2 | a0001c0001t0003g0278 a0001c0001t0003g0279 |
2 | HG02004.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.994+1281C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871165 | |||||||
| chr17:44871174 | C | T | 1 | a0001c0001t0013g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.994+1272G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871174 | |||||||
| chr17:44871267 | C | T | 37 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0008 others(34): Show |
44 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.994+1179G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871267 | |||||||
| chr17:44871390 | A | C | 1 | a0001c0001t0013g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.994+1056T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871390 | |||||||
| chr17:44871495 | C | T | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.994+951G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871495 | |||||||
| chr17:44871508 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.994+938A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871508 | |||||||
| chr17:44871538 | A | G | 41 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0220 others(38): Show |
43 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.994+908T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871538 | |||||||
| chr17:44871558 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.994+888G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871558 | |||||||
| chr17:44871628 | C | T | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.994+818G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871628 | |||||||
| chr17:44871781 | C | T | 2 | a0001c0001t0004g0038 a0001c0001t0004g0057 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.994+665G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871781 | |||||||
| chr17:44871800 | A | T | 80 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(77): Show |
83 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.994+646T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871800 | |||||||
| chr17:44871802 | C | CG | 8 | a0001c0001t0001g0187 a0001c0001t0001g0202 a0001c0001t0001g0220 others(5): Show |
8 | HG00673.hp1 HG00741.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.994+643dupC | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871802 | |||||||
| chr17:44871834 | C | T | 80 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(77): Show |
83 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.994+612G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871834 | |||||||
| chr17:44871953 | T | C | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.994+493A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44871953 | |||||||
| chr17:44872074 | C | T | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.994+372G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44872074 | |||||||
| chr17:44872083 | G | A | 41 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0220 others(38): Show |
43 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.994+363C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44872083 | |||||||
| chr17:44872123 | T | C | 1 | a0001c0001t0004g0051 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.994+323A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44872123 | |||||||
| chr17:44872151 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.994+295A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44872151 | |||||||
| chr17:44872208 | A | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0339 a0001c0001t0001g0340 others(1): Show |
4 | HG02615.hp2 HG02809.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+238T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44872208 | |||||||
| chr17:44872236 | C | T | 3 | a0001c0001t0007g0156 a0001c0001t0007g0158 a0001c0001t0007g0160 |
3 | HG02895.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.994+210G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44872236 | |||||||
| chr17:44872362 | G | A | 1 | a0001c0001t0004g0050 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.994+84C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44872362 | |||||||
| chr17:44872440 | G | A | 80 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(77): Show |
83 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(80): Show |
splice_region_variant&intron_variant | LOW | c.994+6C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 11/27 | chr17 | 44872440 | |||||||
| chr17:44872624 | C | T | 12 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(9): Show |
12 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.870-54G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44872624 | |||||||
| chr17:44872737 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.870-167C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44872737 | |||||||
| chr17:44872749 | C | G | 32 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(29): Show |
33 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.870-179G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44872749 | |||||||
| chr17:44872759 | A | G | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.870-189T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44872759 | |||||||
| chr17:44873085 | C | T | 9 | a0001c0002t0001g0015 a0001c0002t0001g0236 a0001c0002t0001g0237 others(6): Show |
10 | HG00639.hp2 HG01081.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.870-515G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873085 | |||||||
| chr17:44873152 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-582G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873152 | |||||||
| chr17:44873203 | G | A | 1 | a0001c0002t0001g0072 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.870-633C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873203 | |||||||
| chr17:44873214 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.870-644T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873214 | |||||||
| chr17:44873317 | G | A | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.870-747C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873317 | |||||||
| chr17:44873584 | T | C | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.870-1014A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873584 | |||||||
| chr17:44873678 | C | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0339 a0001c0001t0001g0340 others(1): Show |
4 | HG02615.hp2 HG02809.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-1108G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873678 | |||||||
| chr17:44873754 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.870-1184A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873754 | |||||||
| chr17:44873801 | A | G | 93 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(90): Show |
96 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.870-1231T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873801 | |||||||
| chr17:44873817 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-1247G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873817 | |||||||
| chr17:44873818 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870-1248C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873818 | |||||||
| chr17:44873855 | C | T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0134 a0001c0001t0003g0275 |
3 | HG00140.hp2 NA18953.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.870-1285G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873855 | |||||||
| chr17:44873897 | A | G | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.870-1327T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873897 | |||||||
| chr17:44873900 | T | TTTTTTTT others(179): Show |
1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.870-1331_870-1330i others(188): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873900 | |||||||
| chr17:44873907 | G | A | 53 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0008 others(50): Show |
60 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.870-1337C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873907 | |||||||
| chr17:44873920 | G | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-1350C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873920 | |||||||
| chr17:44873924 | T | C | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.870-1354A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873924 | |||||||
| chr17:44873936 | G | T | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.870-1366C>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873936 | |||||||
| chr17:44873976 | C | G | 1 | a0001c0001t0004g0043 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.870-1406G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873976 | |||||||
| chr17:44873977 | G | A | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.870-1407C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873977 | |||||||
| chr17:44873977 | G | C | 1 | a0001c0001t0004g0043 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.870-1407C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44873977 | |||||||
| chr17:44874032 | C | A | 1 | a0001c0001t0004g0029 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.870-1462G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874032 | |||||||
| chr17:44874035 | C | CT | 90 | a0001c0001t0001g0183 a0001c0001t0001g0194 a0001c0001t0001g0195 others(87): Show |
93 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.870-1466dupA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874035 | |||||||
| chr17:44874035 | CT | C | 13 | a0001c0001t0002g0024 a0001c0001t0002g0033 a0001c0001t0002g0106 others(10): Show |
14 | HG00438.hp1 HG01168.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.870-1466delA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874035 | |||||||
| chr17:44874037 | T | C | 1 | a0001c0001t0002g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.870-1467A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874037 | |||||||
| chr17:44874083 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.870-1513G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874083 | |||||||
| chr17:44874161 | C | T | 7 | a0001c0001t0007g0154 a0001c0001t0007g0155 a0001c0001t0007g0156 others(4): Show |
7 | HG02055.hp1 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-1591G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874161 | |||||||
| chr17:44874167 | G | A | 1 | a0001c0001t0003g0296 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870-1597C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874167 | |||||||
| chr17:44874235 | G | C | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.870-1665C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874235 | |||||||
| chr17:44874240 | T | C | 1 | a0001c0001t0004g0046 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.870-1670A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874240 | |||||||
| chr17:44874448 | T | C | 1 | a0001c0002t0001g0323 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.869+1486A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874448 | |||||||
| chr17:44874652 | A | G | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.869+1282T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874652 | |||||||
| chr17:44874788 | A | C | 1 | a0001c0001t0004g0321 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.869+1146T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44874788 | |||||||
| chr17:44875394 | G | A | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.869+540C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44875394 | |||||||
| chr17:44875414 | C | T | 1 | a0001c0001t0004g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.869+520G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44875414 | |||||||
| chr17:44875456 | G | A | 1 | a0001c0001t0005g0250 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.869+478C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44875456 | |||||||
| chr17:44875508 | C | T | 5 | a0001c0001t0003g0260 a0001c0001t0003g0270 a0001c0001t0003g0280 others(2): Show |
5 | HG01169.hp1 HG01891.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+426G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44875508 | |||||||
| chr17:44875700 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.869+234G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44875700 | |||||||
| chr17:44875840 | C | T | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.869+94G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 10/27 | chr17 | 44875840 | |||||||
| chr17:44876390 | C | T | 15 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(12): Show |
17 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.703-290G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876390 | |||||||
| chr17:44876392 | G | A | 1 | a0001c0001t0013g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.703-292C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876392 | |||||||
| chr17:44876427 | T | C | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.703-327A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876427 | |||||||
| chr17:44876450 | T | C | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.703-350A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876450 | |||||||
| chr17:44876522 | G | A | 1 | a0001c0002t0001g0172 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.703-422C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876522 | |||||||
| chr17:44876538 | C | A | 1 | a0001c0001t0002g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.703-438G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876538 | |||||||
| chr17:44876623 | T | C | 83 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(80): Show |
86 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.703-523A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876623 | |||||||
| chr17:44876649 | G | A | 102 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0163 others(99): Show |
112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.703-549C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876649 | |||||||
| chr17:44876760 | G | A | 1 | a0001c0002t0004g0326 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.703-660C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876760 | |||||||
| chr17:44876766 | T | C | 80 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(77): Show |
83 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.703-666A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876766 | |||||||
| chr17:44876797 | G | A | 37 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0008 others(34): Show |
44 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.703-697C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876797 | |||||||
| chr17:44876855 | C | CA | 44 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0092 others(41): Show |
49 | HG00438.hp2 HG00733.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.703-756dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876855 | |||||||
| chr17:44876855 | C | CAA | 34 | a0001c0001t0001g0013 a0001c0001t0001g0093 a0001c0001t0001g0221 others(31): Show |
39 | HG00323.hp2 HG00544.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.703-757_703-756dup others(2): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876855 | |||||||
| chr17:44876855 | C | CAAA | 39 | a0001c0001t0001g0163 a0001c0001t0001g0183 a0001c0001t0001g0191 others(36): Show |
42 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.703-758_703-756dup others(3): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876855 | |||||||
| chr17:44876855 | C | CAAAA | 28 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0177 others(25): Show |
29 | HG00738.hp1 HG01069.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.703-759_703-756dup others(4): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876855 | |||||||
| chr17:44876855 | C | CAAAAA | 58 | a0001c0001t0001g0012 a0001c0001t0001g0179 a0001c0001t0001g0181 others(55): Show |
60 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.703-760_703-756dup others(5): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876855 | |||||||
| chr17:44876855 | C | CAAAAAA | 46 | a0001c0001t0002g0045 a0001c0001t0003g0263 a0001c0001t0003g0264 others(43): Show |
47 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.703-761_703-756dup others(6): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876855 | |||||||
| chr17:44876855 | C | CAAAAAAA | 8 | a0001c0001t0001g0311 a0001c0001t0003g0297 a0001c0001t0003g0309 others(5): Show |
8 | HG01169.hp1 HG02129.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.703-762_703-756dup others(7): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876855 | |||||||
| chr17:44876855 | CAAAAAAA | C | 14 | a0001c0001t0005g0004 a0001c0001t0005g0246 a0001c0001t0005g0247 others(11): Show |
16 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.703-762_703-756del others(7): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876855 | |||||||
| chr17:44876916 | G | C | 1 | a0001c0001t0002g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.703-816C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876916 | |||||||
| chr17:44876972 | T | C | 1 | a0001c0001t0003g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.703-872A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44876972 | |||||||
| chr17:44877003 | C | T | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.703-903G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877003 | |||||||
| chr17:44877074 | T | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(1): Show |
4 | NA18980.hp1 NA18983.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-974A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877074 | |||||||
| chr17:44877129 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.703-1029C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877129 | |||||||
| chr17:44877149 | T | C | 37 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0008 others(34): Show |
44 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.703-1049A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877149 | |||||||
| chr17:44877157 | T | C | 2 | a0001c0001t0001g0311 a0001c0001t0004g0321 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.703-1057A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877157 | |||||||
| chr17:44877317 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.703-1217G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877317 | |||||||
| chr17:44877413 | A | C | 22 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0177 others(19): Show |
24 | HG00642.hp2 HG01069.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.703-1313T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877413 | |||||||
| chr17:44877414 | G | C | 22 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0177 others(19): Show |
24 | HG00642.hp2 HG01069.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.703-1314C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877414 | |||||||
| chr17:44877618 | C | T | 2 | a0001c0002t0001g0007 a0001c0002t0001g0068 |
3 | HG01255.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.703-1518G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877618 | |||||||
| chr17:44877627 | G | A | 1 | a0001c0001t0005g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.703-1527C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877627 | |||||||
| chr17:44877701 | G | GACC | 32 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(29): Show |
33 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.703-1602_703-1601i others(5): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877701 | |||||||
| chr17:44877770 | C | T | 1 | a0001c0001t0005g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.703-1670G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877770 | |||||||
| chr17:44877784 | C | T | 1 | a0001c0002t0001g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.703-1684G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877784 | |||||||
| chr17:44877815 | A | AAAC | 103 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0163 others(100): Show |
113 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.703-1718_703-1716d others(5): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877815 | |||||||
| chr17:44877815 | AAAC | A | 3 | a0001c0001t0002g0140 a0001c0001t0002g0206 a0001c0001t0006g0005 |
4 | HG02109.hp2 HG02148.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-1718_703-1716d others(5): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877815 | |||||||
| chr17:44877815 | AAACAAC | A | 47 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(44): Show |
50 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.703-1721_703-1716d others(8): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877815 | |||||||
| chr17:44877859 | C | T | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.702+1697G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877859 | |||||||
| chr17:44877886 | C | T | 2 | a0001c0001t0003g0278 a0001c0001t0003g0279 |
2 | HG02004.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.702+1670G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877886 | |||||||
| chr17:44877911 | C | G | 1 | a0001c0001t0002g0212 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.702+1645G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877911 | |||||||
| chr17:44877929 | C | G | 2 | a0001c0001t0001g0199 a0001c0001t0013g0166 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.702+1627G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44877929 | |||||||
| chr17:44878091 | G | A | 40 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0163 others(37): Show |
42 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.702+1465C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878091 | |||||||
| chr17:44878104 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0013g0166 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.702+1452G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878104 | |||||||
| chr17:44878221 | T | C | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.702+1335A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878221 | |||||||
| chr17:44878466 | A | G | 1 | a0001c0001t0003g0277 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.702+1090T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878466 | |||||||
| chr17:44878687 | G | A | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.702+869C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878687 | |||||||
| chr17:44878693 | GA | G | 64 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(61): Show |
64 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.702+862delT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878693 | |||||||
| chr17:44878728 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.702+828C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878728 | |||||||
| chr17:44878729 | G | A | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.702+827C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878729 | |||||||
| chr17:44878744 | C | T | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.702+812G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878744 | |||||||
| chr17:44878822 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.702+734C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878822 | |||||||
| chr17:44878841 | A | G | 1 | a0001c0002t0001g0071 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.702+715T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878841 | |||||||
| chr17:44878959 | C | T | 3 | a0001c0001t0007g0156 a0001c0001t0007g0158 a0001c0001t0007g0160 |
3 | HG02895.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.702+597G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44878959 | |||||||
| chr17:44879146 | C | T | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.702+410G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44879146 | |||||||
| chr17:44879167 | C | G | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.702+389G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44879167 | |||||||
| chr17:44879193 | C | T | 4 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0003g0269 others(1): Show |
4 | HG02083.hp2 NA18955.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+363G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44879193 | |||||||
| chr17:44879259 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.702+297A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44879259 | |||||||
| chr17:44879282 | C | T | 41 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0220 others(38): Show |
43 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.702+274G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44879282 | |||||||
| chr17:44879411 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.702+145G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44879411 | |||||||
| chr17:44879430 | T | C | 36 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(33): Show |
37 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.702+126A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 9/27 | chr17 | 44879430 | |||||||
| chr17:44879759 | G | A | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.620-121C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44879759 | |||||||
| chr17:44879766 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0013g0166 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.620-128G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44879766 | |||||||
| chr17:44879771 | C | T | 243 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(240): Show |
258 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.620-133G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44879771 | |||||||
| chr17:44879943 | G | C | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.620-305C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44879943 | |||||||
| chr17:44879959 | G | A | 64 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(61): Show |
64 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.620-321C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44879959 | |||||||
| chr17:44880048 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.620-410A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44880048 | |||||||
| chr17:44880094 | A | G | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.620-456T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44880094 | |||||||
| chr17:44880211 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.619+343G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44880211 | |||||||
| chr17:44880216 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.619+338C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44880216 | |||||||
| chr17:44880263 | T | A | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.619+291A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44880263 | |||||||
| chr17:44880274 | T | C | 41 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0220 others(38): Show |
43 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.619+280A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44880274 | |||||||
| chr17:44880284 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.619+270G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44880284 | |||||||
| chr17:44880487 | A | G | 236 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(233): Show |
251 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.619+67T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44880487 | |||||||
| chr17:44880492 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.619+62A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 8/27 | chr17 | 44880492 | |||||||
| chr17:44880734 | C | T | 1 | a0001c0001t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.529-90G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 7/27 | chr17 | 44880734 | |||||||
| chr17:44880837 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.529-193A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 7/27 | chr17 | 44880837 | |||||||
| chr17:44881006 | T | A | 112 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0177 others(109): Show |
117 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.529-362A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 7/27 | chr17 | 44881006 | |||||||
| chr17:44881007 | A | T | 8 | a0001c0002t0001g0015 a0001c0002t0001g0236 a0001c0002t0001g0237 others(5): Show |
9 | HG00639.hp2 HG01081.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-363T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 7/27 | chr17 | 44881007 | |||||||
| chr17:44881145 | A | C | 1 | a0001c0001t0004g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.529-501T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 7/27 | chr17 | 44881145 | |||||||
| chr17:44881184 | A | G | 243 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(240): Show |
258 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.528+503T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 7/27 | chr17 | 44881184 | |||||||
| chr17:44881290 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.528+397C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 7/27 | chr17 | 44881290 | |||||||
| chr17:44881338 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.528+349G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 7/27 | chr17 | 44881338 | |||||||
| chr17:44881429 | TCTC | T | 39 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0163 others(36): Show |
41 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.528+255_528+257del others(3): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 7/27 | chr17 | 44881429 | |||||||
| chr17:44881778 | G | A | 2 | a0001c0002t0001g0323 a0002c0004t0001g0338 |
2 | HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.493-56C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44881778 | |||||||
| chr17:44881838 | G | A | 1 | a0001c0001t0004g0052 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.493-116C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44881838 | |||||||
| chr17:44881969 | T | C | 5 | a0001c0002t0006g0167 a0001c0002t0006g0168 a0001c0002t0006g0169 others(2): Show |
5 | HG00639.hp2 HG01081.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.493-247A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44881969 | |||||||
| chr17:44881971 | G | A | 2 | a0001c0001t0004g0038 a0001c0001t0004g0057 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.493-249C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44881971 | |||||||
| chr17:44881990 | G | A | 44 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(41): Show |
47 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.493-268C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44881990 | |||||||
| chr17:44882123 | A | G | 114 | a0001c0001t0001g0311 a0001c0001t0002g0033 a0001c0001t0002g0040 others(111): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.493-401T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882123 | |||||||
| chr17:44882179 | C | G | 1 | a0001c0001t0013g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.493-457G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882179 | |||||||
| chr17:44882181 | G | A | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 others(1): Show |
4 | NA18967.hp2 NA18994.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-459C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882181 | |||||||
| chr17:44882211 | G | A | 24 | a0001c0002t0001g0015 a0001c0002t0001g0236 a0001c0002t0001g0237 others(21): Show |
25 | HG00639.hp2 HG01081.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.493-489C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882211 | |||||||
| chr17:44882274 | T | C | 235 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
250 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.493-552A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882274 | |||||||
| chr17:44882370 | G | C | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 others(1): Show |
4 | NA18967.hp2 NA18994.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-648C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882370 | |||||||
| chr17:44882376 | T | G | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 others(1): Show |
4 | NA18967.hp2 NA18994.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-654A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882376 | |||||||
| chr17:44882437 | G | A | 15 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(12): Show |
17 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.492+656C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882437 | |||||||
| chr17:44882555 | G | C | 8 | a0001c0002t0001g0015 a0001c0002t0001g0236 a0001c0002t0001g0237 others(5): Show |
9 | HG00639.hp2 HG01081.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.492+538C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882555 | |||||||
| chr17:44882657 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.492+436A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882657 | |||||||
| chr17:44882774 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.492+319A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882774 | |||||||
| chr17:44882796 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.492+297C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882796 | |||||||
| chr17:44882919 | C | T | 1 | a0001c0001t0004g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.492+174G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 6/27 | chr17 | 44882919 | |||||||
| chr17:44883220 | C | T | 4 | a0001c0001t0003g0265 a0001c0001t0003g0274 a0001c0001t0003g0275 others(1): Show |
4 | HG00140.hp2 HG01943.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-62G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 5/27 | chr17 | 44883220 | |||||||
| chr17:44883256 | G | A | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.427-98C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 5/27 | chr17 | 44883256 | |||||||
| chr17:44883371 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.427-213A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 5/27 | chr17 | 44883371 | |||||||
| chr17:44883393 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.427-235A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 5/27 | chr17 | 44883393 | |||||||
| chr17:44883641 | C | T | 196 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0059 others(193): Show |
209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
splice_region_variant&intron_variant | LOW | c.426+8G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 5/27 | chr17 | 44883641 | |||||||
| chr17:44884129 | G | A | 1 | a0001c0007t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.351-405C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884129 | |||||||
| chr17:44884211 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.351-487G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884211 | |||||||
| chr17:44884280 | C | G | 1 | a0001c0002t0004g0326 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.351-556G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884280 | |||||||
| chr17:44884290 | T | C | 1 | a0001c0005t0003g0266 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.351-566A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884290 | |||||||
| chr17:44884466 | C | T | 1 | a0001c0002t0001g0323 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.351-742G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884466 | |||||||
| chr17:44884475 | T | C | 1 | a0001c0001t0002g0242 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.351-751A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884475 | |||||||
| chr17:44884519 | G | GA | 81 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(78): Show |
83 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.350+736dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884519 | |||||||
| chr17:44884519 | GA | G | 10 | a0001c0001t0001g0013 a0001c0001t0001g0199 a0001c0001t0001g0220 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.350+736delT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884519 | |||||||
| chr17:44884591 | T | C | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.350+665A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884591 | |||||||
| chr17:44884748 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.350+508C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884748 | |||||||
| chr17:44884786 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.350+470G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884786 | |||||||
| chr17:44884798 | C | T | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.350+458G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884798 | |||||||
| chr17:44884926 | T | C | 1 | a0001c0001t0005g0248 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.350+330A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44884926 | |||||||
| chr17:44885200 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0177 others(19): Show |
24 | HG00642.hp2 HG01069.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.350+56G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44885200 | |||||||
| chr17:44885213 | C | G | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.350+43G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 4/27 | chr17 | 44885213 | |||||||
| chr17:44885425 | T | C | 40 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0163 others(37): Show |
42 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.272-91A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44885425 | |||||||
| chr17:44885440 | C | T | 53 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0059 others(50): Show |
55 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.272-106G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44885440 | |||||||
| chr17:44885678 | T | G | 1 | a0001c0001t0002g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.272-344A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44885678 | |||||||
| chr17:44885803 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.272-469A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44885803 | |||||||
| chr17:44885974 | C | T | 1 | a0001c0001t0007g0157 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271+611G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44885974 | |||||||
| chr17:44886044 | C | T | 4 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0003g0269 others(1): Show |
4 | HG02083.hp2 NA18955.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+541G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44886044 | |||||||
| chr17:44886053 | A | G | 7 | a0001c0001t0007g0154 a0001c0001t0007g0155 a0001c0001t0007g0156 others(4): Show |
7 | HG02055.hp1 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+532T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44886053 | |||||||
| chr17:44886131 | G | A | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.271+454C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44886131 | |||||||
| chr17:44886157 | C | T | 2 | a0001c0001t0004g0038 a0001c0001t0004g0057 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.271+428G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44886157 | |||||||
| chr17:44886241 | G | C | 1 | a0001c0001t0003g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.271+344C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44886241 | |||||||
| chr17:44886295 | T | C | 1 | a0001c0001t0003g0273 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.271+290A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 3/27 | chr17 | 44886295 | |||||||
| chr17:44886777 | C | T | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-27G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44886777 | |||||||
| chr17:44886873 | T | C | 5 | a0001c0002t0006g0167 a0001c0002t0006g0168 a0001c0002t0006g0169 others(2): Show |
5 | HG00639.hp2 HG01081.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-123A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44886873 | |||||||
| chr17:44886931 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106-181C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44886931 | |||||||
| chr17:44887038 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0185 a0001c0001t0001g0186 |
4 | HG02258.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-288G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44887038 | |||||||
| chr17:44887095 | A | G | 236 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(233): Show |
251 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.106-345T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44887095 | |||||||
| chr17:44887107 | T | C | 18 | a0001c0001t0001g0163 a0001c0001t0001g0183 a0001c0001t0001g0191 others(15): Show |
18 | HG00621.hp1 HG00639.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.106-357A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44887107 | |||||||
| chr17:44887128 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.106-378A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44887128 | |||||||
| chr17:44887679 | T | G | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-929A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44887679 | |||||||
| chr17:44887810 | C | T | 1 | a0001c0002t0001g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.106-1060G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44887810 | |||||||
| chr17:44887838 | T | C | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.106-1088A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44887838 | |||||||
| chr17:44887858 | T | C | 1 | a0001c0006t0002g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.106-1108A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44887858 | |||||||
| chr17:44888061 | CTACAGG | C | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.106-1317_106-1312d others(8): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888061 | |||||||
| chr17:44888144 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106-1394A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888144 | |||||||
| chr17:44888172 | T | C | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.106-1422A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888172 | |||||||
| chr17:44888173 | G | A | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-1423C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888173 | |||||||
| chr17:44888425 | A | G | 1 | a0001c0001t0002g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.106-1675T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888425 | |||||||
| chr17:44888473 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.106-1723T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888473 | |||||||
| chr17:44888807 | T | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.106-2057A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888807 | |||||||
| chr17:44888854 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.106-2104C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888854 | |||||||
| chr17:44888930 | G | A | 2 | a0001c0002t0001g0011 a0001c0002t0001g0081 |
3 | HG00323.hp2 HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.106-2180C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888930 | |||||||
| chr17:44888932 | C | CATAA | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.106-2186_106-2183d others(6): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44888932 | |||||||
| chr17:44889012 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.106-2262C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44889012 | |||||||
| chr17:44889112 | G | C | 1 | a0001c0002t0001g0090 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.106-2362C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44889112 | |||||||
| chr17:44889118 | G | A | 7 | a0001c0001t0007g0154 a0001c0001t0007g0155 a0001c0001t0007g0156 others(4): Show |
7 | HG02055.hp1 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-2368C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44889118 | |||||||
| chr17:44889119 | G | T | 1 | a0001c0002t0004g0325 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.106-2369C>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44889119 | |||||||
| chr17:44889194 | T | A | 1 | a0001c0001t0004g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.106-2444A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44889194 | |||||||
| chr17:44889569 | C | T | 2 | a0001c0001t0002g0118 a0001c0001t0002g0119 |
2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.106-2819G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44889569 | |||||||
| chr17:44889754 | T | C | 53 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0059 others(50): Show |
55 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.106-3004A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44889754 | |||||||
| chr17:44889927 | T | C | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.106-3177A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44889927 | |||||||
| chr17:44889929 | C | T | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.106-3179G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44889929 | |||||||
| chr17:44890015 | T | A | 1 | a0001c0001t0002g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.106-3265A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890015 | |||||||
| chr17:44890033 | T | G | 1 | a0001c0001t0013g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.106-3283A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890033 | |||||||
| chr17:44890034 | T | A | 1 | a0001c0001t0013g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.106-3284A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890034 | |||||||
| chr17:44890076 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.106-3326G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890076 | |||||||
| chr17:44890125 | A | C | 1 | a0001c0001t0002g0022 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.106-3375T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890125 | |||||||
| chr17:44890131 | T | C | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-3381A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890131 | |||||||
| chr17:44890148 | C | T | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-3398G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890148 | |||||||
| chr17:44890169 | AATTTTTG others(1): Show |
A | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.106-3427_106-3420d others(10): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890169 | |||||||
| chr17:44890201 | A | G | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-3451T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890201 | |||||||
| chr17:44890214 | T | TTCATCAC others(16): Show |
1 | a0001c0001t0002g0023 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.106-3487_106-3465d others(25): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890214 | |||||||
| chr17:44890258 | C | G | 1 | a0001c0001t0002g0117 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.106-3508G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890258 | |||||||
| chr17:44890295 | C | T | 2 | a0001c0001t0005g0252 a0001c0002t0006g0253 |
2 | HG01074.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.106-3545G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890295 | |||||||
| chr17:44890309 | C | T | 2 | a0001c0001t0005g0248 a0001c0001t0012g0020 |
2 | HG01952.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.106-3559G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890309 | |||||||
| chr17:44890323 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.106-3573C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890323 | |||||||
| chr17:44890354 | C | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.106-3604G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890354 | |||||||
| chr17:44890396 | TA | T | 135 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0059 others(132): Show |
140 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.106-3647delT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890396 | |||||||
| chr17:44890397 | A | T | 3 | a0001c0002t0001g0015 a0001c0002t0001g0236 a0001c0002t0001g0237 |
4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-3647T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890397 | |||||||
| chr17:44890398 | A | T | 41 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0220 others(38): Show |
43 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.106-3648T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890398 | |||||||
| chr17:44890399 | A | T | 2 | a0001c0001t0004g0038 a0001c0001t0004g0057 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.106-3649T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890399 | |||||||
| chr17:44890426 | C | G | 1 | a0001c0001t0003g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.106-3676G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890426 | |||||||
| chr17:44890435 | G | A | 1 | a0001c0001t0005g0245 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.106-3685C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890435 | |||||||
| chr17:44890476 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106-3726A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890476 | |||||||
| chr17:44890493 | G | T | 1 | a0001c0001t0007g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.106-3743C>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890493 | |||||||
| chr17:44890552 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-3802G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890552 | |||||||
| chr17:44890638 | G | GC | 17 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(14): Show |
20 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.105+3778dupG | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890638 | |||||||
| chr17:44890700 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.105+3717T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890700 | |||||||
| chr17:44890733 | T | G | 45 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0199 others(42): Show |
47 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.105+3684A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890733 | |||||||
| chr17:44890738 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.105+3679C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890738 | |||||||
| chr17:44890779 | C | T | 2 | a0001c0001t0004g0039 a0001c0001t0004g0043 |
2 | NA19058.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.105+3638G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890779 | |||||||
| chr17:44890974 | C | T | 53 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0059 others(50): Show |
55 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.105+3443G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890974 | |||||||
| chr17:44890999 | C | CTTGG | 32 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(29): Show |
33 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.105+3414_105+3417d others(6): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44890999 | |||||||
| chr17:44891042 | G | A | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.105+3375C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891042 | |||||||
| chr17:44891137 | A | C | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+3280T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891137 | |||||||
| chr17:44891240 | G | A | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.105+3177C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891240 | |||||||
| chr17:44891452 | C | T | 16 | a0001c0002t0001g0323 a0001c0002t0001g0324 a0001c0002t0001g0327 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.105+2965G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891452 | |||||||
| chr17:44891589 | A | G | 7 | a0001c0001t0002g0016 a0001c0001t0002g0238 a0001c0001t0002g0239 others(4): Show |
8 | HG02280.hp1 HG02630.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+2828T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891589 | |||||||
| chr17:44891641 | A | G | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.105+2776T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891641 | |||||||
| chr17:44891645 | T | C | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.105+2772A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891645 | |||||||
| chr17:44891667 | T | A | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.105+2750A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891667 | |||||||
| chr17:44891754 | T | G | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+2663A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891754 | |||||||
| chr17:44891769 | G | A | 5 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0146 others(2): Show |
5 | HG00099.hp1 HG01074.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+2648C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891769 | |||||||
| chr17:44891906 | G | A | 40 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0163 others(37): Show |
42 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.105+2511C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891906 | |||||||
| chr17:44891969 | A | C | 64 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(61): Show |
64 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.105+2448T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44891969 | |||||||
| chr17:44892315 | T | C | 1 | a0001c0002t0001g0089 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.105+2102A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892315 | |||||||
| chr17:44892407 | A | C | 1 | a0001c0001t0003g0274 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.105+2010T>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892407 | |||||||
| chr17:44892452 | T | C | 1 | a0001c0001t0007g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+1965A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892452 | |||||||
| chr17:44892554 | C | A | 2 | a0001c0001t0008g0036 a0001c0001t0008g0037 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.105+1863G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892554 | |||||||
| chr17:44892631 | C | CT | 42 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(39): Show |
42 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.105+1785dupA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892631 | |||||||
| chr17:44892631 | CT | C | 10 | a0001c0001t0001g0339 a0001c0001t0001g0340 a0001c0001t0002g0016 others(7): Show |
12 | HG02280.hp1 HG02615.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+1785delA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892631 | |||||||
| chr17:44892631 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0003g0301 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.105+1773_105+1785d others(15): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892631 | |||||||
| chr17:44892701 | G | A | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.105+1716C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892701 | |||||||
| chr17:44892757 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.105+1660G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892757 | |||||||
| chr17:44892949 | A | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.105+1468T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44892949 | |||||||
| chr17:44893120 | AT | A | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.105+1296delA | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893120 | |||||||
| chr17:44893128 | T | G | 2 | a0001c0001t0001g0199 a0001c0001t0013g0166 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.105+1289A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893128 | |||||||
| chr17:44893132 | T | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0311 a0001c0001t0003g0302 others(3): Show |
6 | HG00642.hp1 HG01515.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+1285A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893132 | |||||||
| chr17:44893271 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.105+1146G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893271 | |||||||
| chr17:44893290 | T | C | 1 | a0001c0001t0002g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.105+1127A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893290 | |||||||
| chr17:44893332 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.105+1085T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893332 | |||||||
| chr17:44893475 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.105+942T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893475 | |||||||
| chr17:44893523 | A | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.105+894T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893523 | |||||||
| chr17:44893544 | C | G | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | HG02602.hp2 HG03654.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+873G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893544 | |||||||
| chr17:44893574 | C | G | 2 | a0001c0001t0001g0199 a0001c0001t0013g0166 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.105+843G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893574 | |||||||
| chr17:44893767 | T | TG | 100 | a0001c0001t0001g0012 a0001c0001t0001g0177 a0001c0001t0001g0178 others(97): Show |
116 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.105+649dupC | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893767 | |||||||
| chr17:44893767 | T | TGG | 26 | a0001c0001t0001g0163 a0001c0001t0001g0192 a0001c0001t0001g0193 others(23): Show |
26 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.105+648_105+649dup others(2): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893767 | |||||||
| chr17:44893767 | TG | T | 31 | a0001c0001t0001g0092 a0001c0001t0002g0040 a0001c0001t0003g0261 others(28): Show |
34 | HG00099.hp2 HG00733.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.105+649delC | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893767 | |||||||
| chr17:44893775 | G | C | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.105+642C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893775 | |||||||
| chr17:44893779 | T | G | 4 | a0001c0001t0001g0218 a0001c0001t0002g0152 a0001c0001t0002g0153 others(1): Show |
4 | HG01070.hp1 HG02300.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+638A>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44893779 | |||||||
| chr17:44894035 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.105+382C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44894035 | |||||||
| chr17:44894067 | C | CA | 96 | a0001c0001t0001g0056 a0001c0001t0001g0311 a0001c0001t0002g0033 others(93): Show |
99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.105+349dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44894067 | |||||||
| chr17:44894067 | C | CAA | 17 | a0001c0001t0002g0040 a0001c0001t0002g0044 a0001c0001t0002g0045 others(14): Show |
18 | HG00438.hp1 HG00609.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.105+348_105+349dup others(2): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44894067 | |||||||
| chr17:44894082 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0006g0005 |
3 | HG02647.hp1 HG02895.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.105+335C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44894082 | |||||||
| chr17:44894198 | T | C | 32 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(29): Show |
33 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.105+219A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44894198 | |||||||
| chr17:44894202 | C | T | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.105+215G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44894202 | |||||||
| chr17:44894205 | G | A | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+212C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44894205 | |||||||
| chr17:44894323 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.105+94A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 2/27 | chr17 | 44894323 | |||||||
| chr17:44894754 | G | A | 7 | a0001c0001t0005g0004 a0001c0001t0005g0251 a0001c0001t0005g0252 others(4): Show |
9 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-229C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44894754 | |||||||
| chr17:44894778 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-4-253A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44894778 | |||||||
| chr17:44894836 | G | A | 2 | a0001c0002t0001g0085 a0001c0002t0001g0086 |
2 | HG00544.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-4-311C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44894836 | |||||||
| chr17:44894838 | G | A | 53 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0059 others(50): Show |
55 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-4-313C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44894838 | |||||||
| chr17:44894926 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-4-401T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44894926 | |||||||
| chr17:44895122 | GGA | G | 17 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(14): Show |
20 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-4-599_-4-598delTC | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895122 | |||||||
| chr17:44895208 | T | C | 1 | a0001c0002t0002g0174 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-4-683A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895208 | |||||||
| chr17:44895223 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4-698G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895223 | |||||||
| chr17:44895280 | G | C | 5 | a0001c0002t0001g0026 a0001c0002t0001g0087 a0001c0002t0001g0088 others(2): Show |
5 | HG00642.hp1 HG00741.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-755C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895280 | |||||||
| chr17:44895322 | G | C | 243 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(240): Show |
258 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.-4-797C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895322 | |||||||
| chr17:44895424 | G | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG01934.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-4-899C>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895424 | |||||||
| chr17:44895495 | C | CA | 8 | a0001c0001t0001g0066 a0001c0001t0001g0200 a0001c0001t0001g0201 others(5): Show |
8 | HG02074.hp1 HG02109.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-971dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895495 | |||||||
| chr17:44895495 | CA | C | 110 | a0001c0001t0001g0163 a0001c0001t0001g0221 a0001c0001t0002g0021 others(107): Show |
120 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-4-971delT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895495 | |||||||
| chr17:44895592 | A | G | 236 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(233): Show |
251 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.-4-1067T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895592 | |||||||
| chr17:44895603 | T | C | 1 | a0001c0001t0004g0321 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-4-1078A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895603 | |||||||
| chr17:44895709 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-4-1184G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895709 | |||||||
| chr17:44895729 | C | G | 1 | a0001c0001t0002g0067 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-4-1204G>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895729 | |||||||
| chr17:44895814 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-1289A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895814 | |||||||
| chr17:44895945 | G | A | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-4-1420C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44895945 | |||||||
| chr17:44896014 | G | A | 3 | a0001c0002t0001g0015 a0001c0002t0001g0236 a0001c0002t0001g0237 |
4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-1489C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896014 | |||||||
| chr17:44896149 | G | C | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-4-1624C>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896149 | |||||||
| chr17:44896182 | T | C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG00639.hp1 HG02004.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-1657A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896182 | |||||||
| chr17:44896422 | C | T | 5 | a0001c0002t0006g0167 a0001c0002t0006g0168 a0001c0002t0006g0169 others(2): Show |
5 | HG00639.hp2 HG01081.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-1897G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896422 | |||||||
| chr17:44896470 | A | G | 1 | a0001c0001t0006g0005 | 2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-4-1945T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896470 | |||||||
| chr17:44896474 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-4-1949G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896474 | |||||||
| chr17:44896602 | G | A | 1 | a0001c0001t0002g0164 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-4-2077C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896602 | |||||||
| chr17:44896698 | C | A | 1 | a0001c0001t0003g0312 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-4-2173G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896698 | |||||||
| chr17:44896775 | C | T | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-4-2250G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896775 | |||||||
| chr17:44896796 | T | C | 1 | a0001c0001t0011g0165 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-4-2271A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896796 | |||||||
| chr17:44896967 | A | G | 1 | a0001c0001t0013g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-5+2402T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896967 | |||||||
| chr17:44896976 | G | A | 1 | a0001c0001t0002g0024 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-5+2393C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44896976 | |||||||
| chr17:44897025 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
10 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+2344C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897025 | |||||||
| chr17:44897076 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5+2293A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897076 | |||||||
| chr17:44897090 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-5+2279G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897090 | |||||||
| chr17:44897215 | C | CA | 74 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): Show |
77 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.-5+2153dupT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897215 | |||||||
| chr17:44897215 | C | CAA | 62 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(59): Show |
62 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-5+2152_-5+2153dup others(2): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897215 | |||||||
| chr17:44897215 | C | CAAA | 9 | a0001c0001t0003g0313 a0001c0001t0003g0314 a0001c0001t0003g0315 others(6): Show |
9 | HG02055.hp2 HG02135.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+2151_-5+2153dup others(3): Show |
EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897215 | |||||||
| chr17:44897215 | CA | C | 9 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(6): Show |
9 | HG00099.hp1 HG01106.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+2153delT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897215 | |||||||
| chr17:44897408 | T | C | 1 | a0001c0001t0012g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5+1961A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897408 | |||||||
| chr17:44897425 | T | C | 1 | a0001c0002t0001g0235 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-5+1944A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897425 | |||||||
| chr17:44897576 | T | A | 1 | a0002c0004t0001g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-5+1793A>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897576 | |||||||
| chr17:44897751 | G | A | 3 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0001c0001t0005g0259 |
3 | HG01891.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-5+1618C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897751 | |||||||
| chr17:44897767 | T | C | 3 | a0001c0002t0001g0015 a0001c0002t0001g0236 a0001c0002t0001g0237 |
4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+1602A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897767 | |||||||
| chr17:44897785 | G | A | 6 | a0001c0001t0002g0016 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
7 | HG02280.hp1 HG02976.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+1584C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897785 | |||||||
| chr17:44897906 | C | A | 1 | a0001c0001t0004g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-5+1463G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897906 | |||||||
| chr17:44897974 | A | T | 1 | a0001c0001t0002g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-5+1395T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897974 | |||||||
| chr17:44897996 | T | C | 1 | a0001c0001t0003g0322 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-5+1373A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44897996 | |||||||
| chr17:44898228 | A | G | 32 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0040 others(29): Show |
33 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-5+1141T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898228 | |||||||
| chr17:44898327 | C | T | 1 | a0001c0001t0004g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+1042G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898327 | |||||||
| chr17:44898335 | A | G | 1 | a0001c0002t0001g0026 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-5+1034T>C | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898335 | |||||||
| chr17:44898661 | G | A | 1 | a0001c0002t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-5+708C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898661 | |||||||
| chr17:44898746 | C | T | 82 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-5+623G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898746 | |||||||
| chr17:44898820 | A | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(1): Show |
4 | NA18980.hp1 NA18983.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+549T>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898820 | |||||||
| chr17:44898827 | CAA | C | 64 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(61): Show |
64 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-5+540_-5+541delTT | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898827 | |||||||
| chr17:44898837 | G | A | 16 | a0001c0001t0005g0004 a0001c0001t0005g0245 a0001c0001t0005g0246 others(13): Show |
18 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-5+532C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898837 | |||||||
| chr17:44898970 | C | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 |
3 | HG01106.hp2 HG01346.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-5+399G>A | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898970 | |||||||
| chr17:44898979 | C | A | 63 | a0001c0001t0001g0311 a0001c0001t0003g0260 a0001c0001t0003g0261 others(60): Show |
63 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-5+390G>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44898979 | |||||||
| chr17:44899172 | G | A | 16 | a0001c0002t0001g0323 a0001c0002t0001g0324 a0001c0002t0001g0327 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5+197C>T | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44899172 | |||||||
| chr17:44899284 | T | C | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-5+85A>G | EFTUD2 | ENSG00000108883.13 | transcript | ENST00000426333.7 | protein_coding | 1/27 | chr17 | 44899284 |